Basic info
Industry
medical equipment manufacturing
Sectors
Medical Device
EU Person Responsible
Cyber Security
Design Control
Diagnostics
Corrective and Preventive Action (CAPA)
Quality Management
Medical Devices
EU Authorised Representative
Machine Learning
Cyber security
Risk Management
IoMT
Regulatory Strategy
Clinical Investigations
Regulatory Affairs
Digital Media
Quality Compliance
Software Validation
Quality Management Systems
EU Legal Representative
SaMD
Product Classification
ISO 13485
Person Responsible for Regulatory Compliance
Artificial Intelligence
Digital Health
Internet of Medical Things
Clinical Evaluations
European Union Authorised Representative
Pharmaceutical
Health Diagnostics
Design Files
Health Care
Technical Files
Date founded
2019